7-[(Substituted-isothioureamethyl)phenyl]-acetamidocephalosporin derivatives

ABSTRACT

Novel cephalosporin derivatives of the following formula are useful as antibacterial agents: ##STR1##

FIELD OF THE INVENTION

This invention relates to novel cephalosporin derivatives useful as antibiotics and processes for their preparation.

SUMMARY OF INVENTION

Compounds of the following general Formula I are useful as antibiotic agents: ##STR2## where Y is hydrogen, chlorine, bromine, a straight or branched lower alkyl group of from 1to 4 carbon atoms, or an alkoxy group of from 1 to 4 carbon atoms; Z is a bond, oxygen or sulfur; W is hydrogen, methyl, amino, hydroxy, SO₃ H, or COOR₄ wherein R₄ is hydrogen or 5-indanyl with the proviso that when Z is oxygen or sulfur, W is other than hydroxy; R₇ is hydrogen or methoxy; each of R₁, R₂, R₃ is hydrogen, amino, formylamino, guanylamino, a straight or branched lower alkyl group of from one to four carbon atoms wherein R₁ and R₂ are a concatenated chain of methylene groups having from three to six methylenes, with the proviso that when R₁ and R₂ are hydrogen and lower alkyl, R₃ is amino, formylamino or guanylamino; R₅ is hydrogen, acetoxy; 1,3,4-thiadiazol-2-ylthio, 5-methyl-1,3,4-thiadiazol-2-ylthio; tetrazol-5-ylthio, 1-methyltetrazol-5-ylthio; 1,3,4-oxadiazol-2-ylthio, 5-methyl-1,3,4-oxadiazol-2-ylthio, 1,2,4-triazol-2-ylthio, 5-methyl-1,3,4-triazol-2-ylthio, 1,2,3-triazol-5-ylthio; R₆ is hydrogen, a cation of an alkali metal or an alkaline earth metal, ammonium or organic ammonium cations, a straight or branched lower alkyl group of from 1 to 4 carbon atoms, a straight or branched alkanoyloxymethyl group in which the alkanoyl moiety has from 2 to 5 carbon atoms and is straight or branched, an alkanoylaminomethyl group in which the alkanoyl moiety is straight or branched and has from 2 to 5 carbon atoms and the amine nitrogen may be substituted with a straight or branched lower alkyl group having from 1 to 4 carbon atoms; an alkoxycarbonylaminomethyl group in which the alkoxy moiety is straight or branched and has from 1 to 4 carbon atoms and the amine nitrogen may be substituted with a straight or branched lower alkyl group of from 1 to 4 carbon atoms, a p-(alkanoyloxy)benzyl group in which the alkanoyl moiety is straight or branched and has from 2 to 5 carbon atoms; an aminoalkanoyloxymethyl group in which the alkanoyl moiety has from 2 to 15 carbon atoms and the amino nitrogen may be mono- or di-substituted with a straight or branched lower alkyl group having from 1 to 4 carbon atoms; and pharmaceutically acceptable salts and individual optical isomers thereof.

The non-toxic acid addition salts of the compounds such as mineral acid addition salts, for example, hydrogen chloride, hydrogen bromide, hydrogen iodide, sulfate, sulfamate and phosphate and organic acid addition salts, for example, maleate, acetate, citrate, oxalate, succinate, benzoate, tartrate, fumarate, malate, mandalate and ascorbate, are also included within the scope of this invention.

DETAILED DESCRIPTION OF INVENTION

In general Formula I the substituent group as represented by R₆ in addition to being hydrogen, a cation or a lower alkyl group may also be alkanoyloxymethyl as represented by the structure: ##STR3## wherein R₈ is selected from a straight or branched lower alkyl group of from 1 to 4 carbon atoms; alkanoylaminolmethyl or alkoxycarbonylaminomethyl as represented by the structure: ##STR4## wherein R₉ represents a straight or branched lower alkyl group of from 1 to 4 carbon atoms or a straight or branched alkoxy group of from 1to 4 carbon atoms, and R₁₀ is selected from hydrogen and a lower alkyl group of from 1 to 4 carbon atoms; p-(alkanoyloxy)benzyl as represented by the structure: ##STR5## wherein R₁₁ is a straight or branched lower alkyl group of from 1to 4 carbon atoms; and aminoalkanoyloxymethyl as represented by the group: ##STR6## wherein m is 0 to 5, each of R₁₂ and R₁₃ is selected from hydrogen or lower alkyl of from 1 to 4 carbon atoms, and each of R₁₄ and R₁₅ is selected from hydrogen or a straight or branched lower alkyl group of from 1 to 4 cabon atoms.

Illustrative examples of straight or branched lower alkyl groups of from 1 to 4 carbon atoms which Y, R₈, R₉, R₁₁, R₁₄ and R₁₅ may represent are methyl, ethyl, n-propyl, isopropyl, n-butyl and tert-butyl.

Examples of lower alkyl groups of from 1 to 4 carbon atoms which R₁₀, R₁₂ and R₁₃ may represent are methyl, ethyl, n-propyl and n-butyl.

Examples of lower alkoxy groups which Y may represent are methoxy, ethoxy, n-propoxy and n-butoxy.

In general Formula I the substitutent group R₅ may represent in addition to hydrogen or acetoxy a heterocyclicthio group selected from 1,3,4-thiadiazol-2-ylthio, 5-methyl-1,3,4-thiadiazol-2-ylthio, tetrazol-5-ylthio, 1-methyltetrazol-5-ylthio, 1,3,4-oxadiazol-12-ylthio, 5-methyl-1,3,4-oxadiazol-2-ylthio, 1,3,4-triazol-2-ylthio, 5-methyl-1,3,4-triazol-2-ylthio and 1,2,3-triazol-5-ylthio as represented by the following respective structures: ##STR7##

Preferred compounds of this invention are those of Formula I wherein W is hydrogen, amino, hydroxy, COOH or SO₃ H. More preferred compounds are those of Formula I wherein W is hydrogen or amino. Another preferred embodiment of this invention are compounds of Formula I wherein Z is a bond as well as compounds wherein Y is hydrogen.

The compounds of Formula I are prepared by treatment of a derivative of Formula II with a derivative of Formula III ##STR8## wherein Y, Z, W, R₁, R₂, R₃, R₅, R₆ and R₇ have the same meaning as described in Formula I and X is a halogen atom such as chlorine, bromine or iodine.

The reaction between a compound of Formula II and a compound of Formula III to give a compound of Formula I takes place when equimolar amounts of the reagents are combined in a suitable solvent. Suitable solvents include, for example, dimethylformamide, acetone, ethyl acetate, acetonitrile, methanol and ethanol. The temperature of the reaction may vary from 0° to 100° C and the reaction time may vary from about 0.5 hour to 10 hours. The product of the reaction of Formula I may be obtained upon removal of the solvent or by precipitation upon combination of the reaction solution with a solvent in which the product is insoluble.

The compounds of Formula II may be used in situ without the need of prior isolation when prepared by coupling a compound of Formula IV with an acid of formula V or a functional equivalent thereof ##STR9## wherein R₅, R₆, R₇, X, Y, Z and W are as described above.

Compounds of Formulas II and V have been described in U.S. Pat. Nos. 3,919,206, 3,948,904 and4,026,887. Compounds of Formula III are commercially available or may be readily prepared by known procedures.

The compounds of general Formula IV, that is, 7-aminocephalosporanic acid and 7-aminodesacetoxycephalosporanic acid and derivatives thereof are commercially available or may be obtained from Penicillin G, cephalosporin C or cephamycin C by processes known in the art. For example compounds of Formula IV wherein R₇ is methoxy may be prepared as described by M. Sletzinger, et al., J. Am. Chem. Soc., 94, 1408 (1972). Compounds of Formula IV may also be prepared as described in U.S. Pat. Nos. 3,948,904 and 4,026,887.

When the substituent group W in the above Formula V represents an amino group suitable blocking groups, for example, tert-butoxycarbonyl, or carbobenzyloxy are employed to protect the amino function. Such blocking groups are removed after the coupling reaction by methods generally known in the art, for example, as described by Lemieux, et al., in U.S. Pat. No. 3,657,232.

The preparation of a compound of Formula V wherein W is --COOindanyl may be carried out by reacting the corresponding compound of Formula V wherein W is --COOH with 1 mole of 5-indanol in an inert solvent such as chloroform, dichloromethane, dimethylformamide, in the presence of N,N'-dicyclohexylcarbodiimide at a pH of about 2.5 and a temperature of from 20° to 30° C. The product is isolated upon filtration of the N,N'-dicyclohexylurea formed and subsequent removal of the solvent.

Functional equivalents of the acids as represented by Formula V include the acid halides, for example, the acid chloride, acid anhydrides, including mixed anhydrides with, for example, alkylphoshoric acids, lower aliphatic monoesters of carbonic acid, or alkyl or aryl sulfonic acids. Additionally, the acid azide or an active ester or thioester, for example, with p-nitrophenol, 2,4-dinitrophenol, or thioacetic acid, may be used, or the free acid as represented by Formula V may be coupled with the 7-aminocephalosporanic acid derivative as represented by Formula IV after first reacting the acid with N,N'-dicylcohexylcarbodiimide, or N-cyclohexyl-N'-(2-morpholinoethyl)carbodiimide.

The coupling reaction between compounds of Formula IV and Formula V is generally carried out in the presence of a solvent such as ethyl acetate, acetone, dioxane, acetonitrile, chloroform, ethylene chloride, tetrahydrofuran and dimethylformamide and optionally in the presence of a base such as sodium bicarbonate, triethylamine or N,N-dimethylaniline. The temperature of the reaction may vary from -10° to 100° C, and the reaction time may vary from about 1/2 hour to 10 hours. The cephalosporin products are isolated by conventional methods.

The salt forms of Formula I wherein R is a pharmaceutically acceptable cation are prepared in the manner recognized in the art and may be formed in situ or by reacting the corresponding acid with base, for example, sodium bicarbonate or triethylamine.

The compounds of Formula I wherein R₅ is selected from a heteroarylthiol residue may also be prepared by the reaction of a compound of Formula I wherein R₅ is acetoxy namely Formula VI with an appropriate heteroarylthiol of Formula VII as schematically described below: ##STR10## Wherein X, Y, W, Z, R₇ and R₆ are as described above, and R₁₆ is a heteroarylthio residue selected from 1,3,4-thiadiazol-2-ylthio, 5-methyl-1,3,4-thiadiazol-2-ylthio, tetrazol-5-ylthio, 1-methyltetrazol-5-ylthio, 1,3,4-oxadiazol-2-ylthio, 5-methyl-1,3,4-oxadiazol-2-ylthio, 1,3,4-triazol-2-ylthio, 5-methyl-1,3,4-triazol-2-ylthio, and 1,2,3-triazol-5-ylthio.

The reaction is generally carried out in the presence of a solvent. Suitable solvents include water, methanol, ethanol, dimethylformamide and dimethylsulfoxide. The reaction is carried out by mixing in a suitable solvent a compound of Formula VI with a compound of Formula VII, in such a way that the compound of Formula VII may be present in a non-stoichiometric excess relative to the compound of Formula VI. The reaction temperature may vary from about 25° to 100° C and the reaction time may vary from about 0.5 hour to 10 hours. The reaction may be carried out in the presence of a base such as sodium carbonate, sodium bicarbonate or triethylamine. The product of the reaction is isolated by conventional methods known in the art.

The individual optical isomers of the compounds of general Formula I wherein W represents methyl, amino, hydroxy, COOR₄ or SO₃ H are also included within the scope of this invention.

The novel compounds of this invention are useful as antibiotic agents as demonstrated by their activity against gram positive and gram negative bacteria in vitro and fungi. The compounds of this invention are particularly useful in that they possess a longer duration of activity than many of the well known cephalosporin compounds. Illustrative examples of bacteria against which the compounds of this invention are active are Staphylococcus aureus, Salmonella schottmulleri, Klebsiella pneumonia, Diplococcus pneumonia and Streptococcus pyrogenes.

The compounds of this invention may be administered alone or in the form of pharmaceutical preparations either orally, parenterally and topically. They may be administered to warm blooded animals, that is, birds and mammals, for example felines, canines, bovines, and equines and humans. For oral administration the compounds may be administered in the form of tablets, capsules or pills or in the form of elixirs or suspensions. For parenteral administration they are best used in the form of a sterile aqueous solution which may contain other solutes, for example, enough saline or glucose to make the solution isotonic. For topical administration the compounds may be incorporated into creams or ointments.

GENERAL PROCEDURES FOR THE PREPARATION OF COMPOUNDS OF FORMULA I PROCEDURE I

To a solution of a compound of Formula II in 5-10 ml of dimethylformamide an equimolar amount of a compound of Formula III is added. The solution is stirred at about 25° C for 30 minutes and at 55° C for 3 hours, and is then added to 200 ml of dichloromethane. The mixture is stirred for 30 minutes. The precipitated solid is filtered, washed with dichloromethane, and dried to give the product isolated as the hydrohalide salt.

PROCEDURE II

To a cold solution of sodium bicarbonate (2 equivalents) and a compound of Formula IV (1 equivalent) in a mixture of 3 parts of water to 2 parts of acetone is added a compound of Formula V in one part of acetone. The solution is stirred for 30 minutes at about 25° C and is then flash concentrated until all the acetone has been removed. To the obtained solution a compound of Formula III (1 equivalent) is added. The solution is stirred at about 25° C for 2 hours. During this time a solid precipitate is formed which is filtered, washed with water and dried to give the desired compound of Formula I.

EXAMPLE 1 3-[(Acetyloxy)methyl]-7-[[[4-[[(amino-hydroazonomethyl)-thio]methyl]phenyl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid hydrochloride

The title compound is obtained in 67% yield when prepared according to Procedure I when the reagents are 3-[(acetyloxy)methyl]-7-[[2-[4-(chloromethyl)phenyl]-acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (a compound of Formula II) and thiosemicarbazide (a compound of Formula III).

NMR (DMSO-D₆ +D₂ O) ppm (δ), 2.10 (s,3), 3.6 (broad s,2), 4.5 (broad s,2), 4.92 (q,2), 5.14 (d,1), 5.70 (d,1), 7.37 (s,4).

When in the procedure of Example 1 an appropriate amount of a chloromethyl substituted cephalosporin of Formula II listed in the following Table I is substituted for 3-[(acetyloxy)methyl]-7-[[2-[4-(chloromethyl)phenyl]-acetyl]amino]-8 -oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid and an appropriate amount of a compound of Formula III listed in the following Table I is substituted for thiosemicarbazide the respective 7-[[[(substituted isothiourea)methyl]phenyl]acetyl]cephalosporin product listed in Table I is obtained.

                                      TABLE I                                      __________________________________________________________________________     Chloromethyl Substituted                                                                        Reagent of                                                                            Substituted                                            Cephalosporin Derivative                                                                        Formula III                                                                           Cephalosporin Product                                  __________________________________________________________________________     3-[(1-Methyltetrazol-5-ylthio)-                                                                 Ethylene-                                                                             7-[[[4-[[(4,5-Dihydro-1H-                              methyl]-7-[[2-[4-(chloromethyl)-                                                                thiourea                                                                              imidazol-2-yl)thio]methyl]-                            phenyl]-2-hydroxyacetyl]amino]-                                                                        phenyl]hydroxyacetyl]amino]-                           8-oxo-5-thia-1-azabicyclo-                                                                             3-[[(1-methyl-1H-tetrazol-5-                           [4.2.0.]oct-2-ene-2-carboxylic                                                                         yl)thio]methyl]-8-oxo-5-thia-                          acid                    1-azabicyclo[4.2.0]oct-2-ene-                                                  2-carboxylic acid                                      3-[(Acetyloxy)methyl]-7-[[2-[4-                                                                 Thiosemi                                                                              3-[(Acetyloxy)methyl]-7-[[[4-                          (chloromethyl)phenyl]-2-carboxy-                                                                carbazide                                                                             [[(aminohydrazonomethyl]thio]-                         actyl]amino]-8-oxo-5-thia-1-                                                                           methyl]phenyl]carboxyacetyl]-                          azabicyclo[4.2.0]oct-2-ene-2-                                                                          amino]-8-oxo-5-thia-1-azabi-                           carboxylic acid         cyclo[4.2.0]oct-2-ene-2-                                                       carboxylic acid                                        7-[[2-[4-(chloromethyl)phenyl]-                                                                 Formylthio-                                                                           7-[[[4-[[[Amino(formylhydra-                           2-sulfoacetyl]amino]-3-[(1,3,4-                                                                 semi-  zono)methyl]thio]methyl]-                              thiadiazol-5-ylthio)methyl]-                                                                    carbazide                                                                             phenyl]sulfoacetyl]amino]-3-                           8-oxo-5-thia-1-azabicyclo-                                                                             [[(1,3,4-thiadiazol-2-yl)thio]-                        [4.2.0]oct-2-ene-2-carboxylic                                                                          methyl]-8-oxo-5-thia-1-azabi-                          acid                    cyclo[4.2.0]oct-2-ene-2-car-                                                   boxylic acid                                           3-[(Acetyloxy)methyl]-7-[[2-[4-                                                                 Formylthio-                                                                           3-[(Acetyloxy)methyl]-7-[[[4-                          (chloromethyl)phenoxy]acetyl]-                                                                  semi-  [[[amino(formylhydrazono)-                             amino]-8-oxo-5-thia-1-azabicyclo-                                                               carbazide                                                                             methyl]thio]methyl]phenyl]-                            [4.2.0]oct-2-ene-2-carboxylic                                                                          acetyl]amino]-8-oxo-5-thia-1-                          acid                    azabicyclo[4.2.0]oct-2-ene-2-                                                  carboxylic acid                                        3-[(Acetyloxy)methyl]-7-[[2-                                                                    Thiosemi-                                                                             7-[[[4-[[(Aminohydrazonomethyl)-                       [2-(chloro)-4-(chloromethyl)-                                                                   carbazide                                                                             thio]methyl]-2-chlorophenyl]-                          phenyl]acetyl]amino]-8-oxo-5-                                                                          acetyl]amino]-3-[(acetyloxy)-                          thia-1-azabicyclo[4.2.0]oct-2-                                                                         methyl]-8-oxo-5-thia-1-azabi-                          ene-2-carboxylic acid   cyclo[4.2.0]oct-2-ene-2-car-                                                   boxylic acid                                           3-[(Acetyloxy)methyl]-7-[[2-                                                                    Guanyl-                                                                               7-[[Amino[4-[[[amino[(amino-                           [4-(chloromethyl)phenyl]-2-                                                                     thiourea                                                                              iminomethyl)imino]methyl]thio]-                        aminoacetyl]amino]-8-oxo-5-                                                                            methyl]phenyl]acetyl]amino]-3-                         thia-1-azabicyclo[4.2.0]oct-2-                                                                         acetyloxymethyl-8-oxo-5-thia-1-                        ene-2-carboxylic acid 2,2-                                                                             azabicyclo[4.2.0]oct-2-ene-2-                          dimethyl-1-oxopropoxymethyl                                                                            carboxylic acid, (2,2-dimethyl-                        ester                   1-oxopropoxy)methyl ester                              3-[(1,3,4-Thiadiazol-5-ylthio)-                                                                 Guanyl-                                                                               7-[[[4-[[[Amino[(aminoimino-                           methyl]-7-[[2-[4-(chloromethyl)-                                                                thiourea                                                                              methyl)imino]methyl]thio]-                             phenoxy]acetyl]amino]-8-oxo-5-                                                                         methyl]phenoxy]acetyl]amino]-                          thia-1-azabicyclo[4.2.0]oct-2-                                                                         8-oxo-3-[(1,3,4-thiadiazol-5-                          ene-2-carboxylic acid   ylthio)methyl]-5-thia-1-azabi-                                                 cyclo[4.2.0]oct-2-ene-2-                                                       carboxylic acid                                        __________________________________________________________________________

EXAMPLE 2 7-[[[4-[[(Aminohydroazonomethyl)]methyl]phenyl]acetyl]-amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

The title compound is obtained in 42% yield when prepared according to Procedure II when the reagents used are 3-(1-methyltetrazolyl-5-thio)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (a compound of Formula IV) p-chloromethylphenylacetyl chloride (a compound of Formula V) and thiosemicarbazide (a compound of Formula III).

NMR (DMSO-D₆ +D₂ O) ppm (δ), 3.5 (broad s,2), 3.95 (s,3), 4.3 (broad s,2), 5.02 (d,1), 5.6 (d,1), 7.3 (m,4).

EXAMPLE 3 7-[[[4-[[[Amino(formylhydrazono)methyl]thio]methyl]phenyl]-acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

The title compound is obtained in 36% yield as described in Example 2, when an appropriate amount of formylthiosemicarbazide is used instead of thiosemicarbazide.

NMR (DMSO-D₆ +D₂ O), ppm (δ), 3.5 (broad s,2), 3.9 (s, 3), 4.3 (broad s,2), 5.07 (d,1), 5.7 (d,1), 7.3 (s,4), 8.0 (s,1).

EXAMPLE 4 7-[[[4-[[[Amino[(aminominomethyl)imino]methyl]thio]-methyl]phenyl]acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

The title compound is obtained in 80% yield as described in Example 2 when an appropriate amount of guanylthiourea is used instead of thiosemicarbazide. NMR (DMSO-D₆ +D₂ O), ppm (δ) 3.6 (broad s,2), 3.97 (s,3), 4.32 (broad s,2), 5.05 (d,1), 5.65 (d,1), 7.35 (s,4).

EXAMPLE 5 7-[[[4-[[(4,5-Dihydro-1H-imidazol-2-yl)thio]methyl]-phenyl]acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]-methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

The title compound is obtained in 44% yield as described in Example 2 by replacing thiosemicarbazide with an appropriate amount of ethylene thiourea.

NMR (DMSO-D₆ +D₂ O), ppm (δ), 2.5 (broad s,4), 3.6 (broad s,2), 3.01 (s,3), 4.33 (broad s,2), 4.55 (s,2), 5.0 (d,1), 5.6 (d,1), 7.4 (broad s,4). 

We claim:
 1. A compound of the formula ##STR11## wherein Y is hydrogen, chlorine, bromine, a straight or branched lower alkyl group of from 1 to 4 carbon atoms, or an alkoxy group of from 1 to 4 carbon atoms; Z is a bond, oxygen or sulfur; W is hydrogen, methyl, amino, hydroxy, --SO₃ H or --COOR₄ wherein R₄ is hydrogen or 5-idanyl with the proviso that when Z is oxygen or sulfur, W is other than hydroxy; R₇ is hydrogen or methoxy; each of R₁, R₂ R₃ is hydrogen, amino, formylamino, guanylamino, a straight or branched lower alkyl group of from 1 to 4 carbon atoms, wherein R₁ and R₂ are a concatenated chain of methylene groups having from 3 to 6 methylenes, with the proviso that when R₁ and R₂ are hydrogen or lower alkyl, R₃ is amino, formylamino or guanylamino; R₅ is 1,3,4-thiadiazol-2-ylthio, 5-methyl-1,3,4-thiadiazol-2-ylthio, tetrazol-5-ylthio, 1-methyltetrazol-5-ylthio, 1,3,4-oxadiazol-2-ylthio, 5-methyl-1,3,4-oxadiazol-2-ylthio, 1,3,4-triazol-2-ylthio, 5-methyl-1,3,4-triazol-2-ylthio or 1,2,3-triazol-5-ylthio; R₆ is hydrogen; a cation of an alkali metal or an alkaline earth metal, ammonium a straight or branched lower alkyl group of from 1 to 4 carbon atoms, a straight or branched alkanoyloxymethyl group in which the alkanoyl moiety has from 2 to 5 carbon atoms and is straight or branched, an alkanoylaminomethyl group in which the alkanoyl moiety is straight or branched and has from 2 to 5 carbon atoms and the amine nitrogen may be substituted with a straight or branched lower alkyl group having 1 to 4 carbon atoms; an alkoxycabonylaminomethyl group in which the alkoxy moiety is straight or branched and has from 1 to 4 carbon atoms and the amine nitrogen may be substituted with a straight or branched lower alkyl group of from 1 to 4 carbon atoms, a p-(alkanoyloxy)-benzyl group in which the alkanoyl moiety is straight or branched and has from 2 to 5 carbon atoms; an aminoalkanoyloxymethyl group in which the alkanoyl moiety has from 2 to 15 carbon atoms and the amino nitrogen may be mono- or di-substituted with a straight or branched lower alkyl group having from 1 to 4 carbon atoms; and pharmaceutically acceptable salts and individual optical isomers thereof.
 2. A compound of claim 1 wherein W is selected from hydrogen, amino, hydroxy, CO₂ H, SO₃ H.
 3. A compound of claim 2 wherein Z is a bond.
 4. A compound of claim 3 wherein Y is hydrogen.
 5. A compound of claim 4 which is 7-[[[4-[[(aminohydrazonomethyl)thio]methyl]phenyl]acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid or a pharmaceutically acceptable salt thereof.
 6. A compound of claim 4 which is 7-[[[4-[[[amino(formylhydrazono)methyl]thio]methyl]phenyl]acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid or a pharmaceutically acceptable salt thereof.
 7. The compound 7-[[[4-[[(4,5-dihydro-1H-imidazol-2-yl)-thio]methyl]phenyl]acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. 